Photoinduced decatungstate-catalyzed C(sp)-H thioetherification by sulfinate salts
Thiols and thioesters play crucial roles in pharmaceuticals, biology, and material science as essential organosulfur compounds. Leveraging readily available and cost-effective inert alkanes through direct thioetherification holds promise for yielding high-value-added products. Herein, we present a p...
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Veröffentlicht in: | Organic & biomolecular chemistry 2024-05, Vol.22 (17), p.342-3424 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Thiols and thioesters play crucial roles in pharmaceuticals, biology, and material science as essential organosulfur compounds. Leveraging readily available and cost-effective inert alkanes through direct thioetherification holds promise for yielding high-value-added products. Herein, we present a photoinduced strategy for sulfur-containing modification of inert alkanes utilizing decatungstate as hydrogen atom transfer reagent, offering a straightforward and practical approach for synthesizing thioethers and thioesters.
A visible light photoinduced decatungstate-catalyzed C(sp
3
)-H thioetherification of hydrocarbons by sodium sulfite is herein reported. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/d4ob00394b |